Katalin Csiszar to Williams Syndrome
This is a "connection" page, showing publications Katalin Csiszar has written about Williams Syndrome.
Connection Strength
0.267
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Urb?n Z, Peyrol S, Plauchu H, Zabot MT, Lebwohl M, Schilling K, Green M, Boyd CD, Csisz?r K. Elastin gene deletions in Williams syndrome patients result in altered deposition of elastic fibers in skin and a subclinical dermal phenotype. Pediatr Dermatol. 2000 Jan-Feb; 17(1):12-20.
Score: 0.181
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del Rio T, Urb?n Z, Csisz?r K, Boyd CD. A gene-dosage PCR method for the detection of elastin gene deletions in patients with Williams syndrome. Clin Genet. 1998 Aug; 54(2):129-35.
Score: 0.041
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Urb?n Z, Helms C, Fekete G, Csisz?r K, Bonnet D, Munnich A, Donis-Keller H, Boyd CD. 7q11.23 deletions in Williams syndrome arise as a consequence of unequal meiotic crossover. Am J Hum Genet. 1996 Oct; 59(4):958-62.
Score: 0.036
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Urb?n Z, Csisz?r K, Fekete G, Boyd CD. A tetranucleotide repeat polymorphism within the human elastin gene (ELNi1). Clin Genet. 1997 Feb; 51(2):133-4.
Score: 0.009